Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance

ABSTRACT Stenotrophomonas maltophilia is responsible for a growing number of nosocomial infections and is difficult to treat owing to limited antibiotic susceptibilities. However, there are numerous recently published examples where traditional susceptibility testing methodology fails to accurately...

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Main Authors: Matthew C. Phillips, Bosul Lee, Sarah L. Miller, Jun Yan, Kristine Goy, Marlène Maeusli, Tina Lam, Catherine Spellberg, Michael Spellberg, Rosemary She, Brad Spellberg, Brian Luna
Format: Article
Language:English
Published: American Society for Microbiology 2025-06-01
Series:mSphere
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Online Access:https://journals.asm.org/doi/10.1128/msphere.00840-24
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author Matthew C. Phillips
Bosul Lee
Sarah L. Miller
Jun Yan
Kristine Goy
Marlène Maeusli
Tina Lam
Catherine Spellberg
Michael Spellberg
Rosemary She
Brad Spellberg
Brian Luna
author_facet Matthew C. Phillips
Bosul Lee
Sarah L. Miller
Jun Yan
Kristine Goy
Marlène Maeusli
Tina Lam
Catherine Spellberg
Michael Spellberg
Rosemary She
Brad Spellberg
Brian Luna
author_sort Matthew C. Phillips
collection DOAJ
description ABSTRACT Stenotrophomonas maltophilia is responsible for a growing number of nosocomial infections and is difficult to treat owing to limited antibiotic susceptibilities. However, there are numerous recently published examples where traditional susceptibility testing methodology fails to accurately predict in vivo efficacy. We sought to determine if there were efficacious antibiotics against S. maltophilia that have been overlooked due to specious in vivo resistance determined by traditional in vitro methods. Antibiotic resistance testing was performed utilizing conventional and nutrient-limited media. Antibiotics with discordant minimum inhibitory concentrations (MICs) between the two media were selected for further experimentation. Metal ions were supplemented back into the nutrient-limited media to establish possible mechanisms. In vivo corroborations of in vitro MICs were done utilizing two infection models, Galleria mellonella and a neutropenic mouse oral aspiration pneumonia model. S. maltophilia MICs were significantly lower for ceftazidime in nutritionally deficient media that better corresponds to the in vivo environment than conventional rich media, resulting in a high percentage of strains determined resistant in traditional media being determined susceptible in nutritionally deficient media. The addition of zinc and manganese to the deficient media abrogated this difference, which was dependent on the L1 metallo-β-lactamase (MBL). Ceftazidime protected both G. mellonella and neutropenic mice against lethal infection caused by S. maltophilia that was predicted to be resistant in traditional media but susceptible in nutrient-deficient media. Ceftazidime may remain a viable therapeutic option for patients with S. maltophilia infection caused by strains predicted to be resistant by traditional susceptibility testing. Sequestration of trace metals in the host environment may prevent S. maltophilia MBL activity against ceftazidime.IMPORTANCEBreakpoint interpretation criteria for ceftazidime against S. maltophilia were recently removed by CLSI and the FDA. It was noted that clinical data were insufficient to validate the current breakpoints. Clinical data were mixed, with some studies reporting treatment success, but others reporting treatment failure. We believe that antimicrobial testing is suboptimal, and improved testing strategies, such as the use of zinc-limited media for culture, will better model the activity of ceftazidime in vitro. Improved susceptibility testing strategies may better discriminate against those isolates that are truly resistant from those that were previously falsely identified as being resistant using conventional testing methods.
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spelling doaj-art-6b0e17cabcbc4d75a394b2ca296efeb42025-08-20T03:30:25ZengAmerican Society for MicrobiologymSphere2379-50422025-06-0110610.1128/msphere.00840-24Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistanceMatthew C. Phillips0Bosul Lee1Sarah L. Miller2Jun Yan3Kristine Goy4Marlène Maeusli5Tina Lam6Catherine Spellberg7Michael Spellberg8Rosemary She9Brad Spellberg10Brian Luna11Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USADepartment of Pathology, City of Hope, Duarte, California, USALos Angeles General Hospital, Los Angeles, California, USADepartment of Molecular Microbiology and Immunology, Keck School of Medicine at USC, Los Angeles, California, USAABSTRACT Stenotrophomonas maltophilia is responsible for a growing number of nosocomial infections and is difficult to treat owing to limited antibiotic susceptibilities. However, there are numerous recently published examples where traditional susceptibility testing methodology fails to accurately predict in vivo efficacy. We sought to determine if there were efficacious antibiotics against S. maltophilia that have been overlooked due to specious in vivo resistance determined by traditional in vitro methods. Antibiotic resistance testing was performed utilizing conventional and nutrient-limited media. Antibiotics with discordant minimum inhibitory concentrations (MICs) between the two media were selected for further experimentation. Metal ions were supplemented back into the nutrient-limited media to establish possible mechanisms. In vivo corroborations of in vitro MICs were done utilizing two infection models, Galleria mellonella and a neutropenic mouse oral aspiration pneumonia model. S. maltophilia MICs were significantly lower for ceftazidime in nutritionally deficient media that better corresponds to the in vivo environment than conventional rich media, resulting in a high percentage of strains determined resistant in traditional media being determined susceptible in nutritionally deficient media. The addition of zinc and manganese to the deficient media abrogated this difference, which was dependent on the L1 metallo-β-lactamase (MBL). Ceftazidime protected both G. mellonella and neutropenic mice against lethal infection caused by S. maltophilia that was predicted to be resistant in traditional media but susceptible in nutrient-deficient media. Ceftazidime may remain a viable therapeutic option for patients with S. maltophilia infection caused by strains predicted to be resistant by traditional susceptibility testing. Sequestration of trace metals in the host environment may prevent S. maltophilia MBL activity against ceftazidime.IMPORTANCEBreakpoint interpretation criteria for ceftazidime against S. maltophilia were recently removed by CLSI and the FDA. It was noted that clinical data were insufficient to validate the current breakpoints. Clinical data were mixed, with some studies reporting treatment success, but others reporting treatment failure. We believe that antimicrobial testing is suboptimal, and improved testing strategies, such as the use of zinc-limited media for culture, will better model the activity of ceftazidime in vitro. Improved susceptibility testing strategies may better discriminate against those isolates that are truly resistant from those that were previously falsely identified as being resistant using conventional testing methods.https://journals.asm.org/doi/10.1128/msphere.00840-24gram-negative bacteriaantibiotic resistancebeta-lactamasesbeta-lactamsStenotrophomonas
spellingShingle Matthew C. Phillips
Bosul Lee
Sarah L. Miller
Jun Yan
Kristine Goy
Marlène Maeusli
Tina Lam
Catherine Spellberg
Michael Spellberg
Rosemary She
Brad Spellberg
Brian Luna
Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
mSphere
gram-negative bacteria
antibiotic resistance
beta-lactamases
beta-lactams
Stenotrophomonas
title Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
title_full Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
title_fullStr Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
title_full_unstemmed Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
title_short Ceftazidime retains in vivo efficacy against strains of Stenotrophomonas maltophilia for which traditional testing predicts resistance
title_sort ceftazidime retains in vivo efficacy against strains of stenotrophomonas maltophilia for which traditional testing predicts resistance
topic gram-negative bacteria
antibiotic resistance
beta-lactamases
beta-lactams
Stenotrophomonas
url https://journals.asm.org/doi/10.1128/msphere.00840-24
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